Disease #05671 (FNSS2 (sleep, short, natural, familial, type 2 (FNSS2)), OMIM:618591)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FNSS2
Name	sleep, short, natural, familial, type 2 (FNSS2)
OMIM ID	618591
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ADRB1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2019-11-04 08:47:56 +01:00 (CET)
Date last edited	N/A

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